Topical diclofenac patch

ABSTRACT

The invention provides an analgesic anti-inflammatory patch of a hydrophobic type for topical application containing, in a Pressure Sensitive Adhesive (PSA), diclofenac sodium, pyrrolidone or a derivative thereof, a polyhydric alcohol fatty acid ester, and an organic acid. The patch exerts the following effects:
         (1) diclofenac sodium is effectively and continuously released from a Pressure Sensitive Adhesive (PSA) and percutaneously absorbed, thereby attaining sustained, excellent pharmaceutical and pharmacological effects;   (2) the patch per se has high tackiness and safety; and   (3) diclofenac sodium remains stable in the Pressure Sensitive Adhesive (PSA).

TECHNICAL FIELD

The present invention relates to a patch containing diclofenac sodium asan active ingredient, the patch exhibiting excellent releasability andpercutaneous absorbability of diclofenac sodium and exerting a stableanalgesic anti-inflammatory effect for a long period of time upontopical application.

BACKGROUND ART

Diclofenac sodium exerts excellent antipyretic, analgesic, andanti-inflammatory effects. Drug preparations containing diclofenacsodium are generally divided into peroral drugs exhibiting a systemicaction and drugs for external use exhibiting a topical action. When aperoral drug is administered, grave, systemic adverse effects such asgastrointestinal disorders occur, thereby calling for furtherdevelopment of percutaneous-absorption-type patches for topicalapplication for mitigating such adverse effects. In connection with apatch containing a non-steroidal analgesic anti-inflammatory drug suchas diclofenac sodium, the most important issues are effective, sustainedpercutaneous absorption of the active ingredient into the disturbedportion directly under the patch and delivery of the active ingredientto the disturbed portion directly under the patch.

Since diclofenac sodium has considerably low solubility in water and anoily component, a wide range of studies have been carried out in orderto stabilize it in a dissolved state in a drug for external use forpromoting percutaneous absorption from a patch. For example, JapanesePatent Application Laid-Open (kokai) No. 61-280426 disclosesincorporation of an organic acid (citric acid) as an additive forenhancing the solubility and percutaneous absorbability of diclofenacsodium. Japanese Patent Application Laid-Open (kokai) No. 4-193826discloses incorporation of an essential oil component such as menthol ormentha oil as a percutaneous absorption promoter for diclofenac sodium.Japanese Patent Application Laid-Open (kokai) No. 5-178763 disclosesincorporation of a polyhydric alcohol medium-chain fatty acid ester as asolubilizer for slightly soluble drugs. Japanese Patent ApplicationLaid-Open (kokai) No. 11-222443 discloses incorporation of 1-menthol anda pyrrolidone (pyrrolidone or at least one derivative thereof) as apercutaneous absorption promoter for diclofenac sodium.

However, percutaneous absorbability of a drug containing diclofenacsodium for external use is still unsatisfactory, and thus, there stillremains a need for a drug for external use which promises more effectivepercutaneous absorption.

Thus, an object of the present invention is to provide a patch whichexhibits excellent releasability and percutaneous absorbability ofdiclofenac sodium.

DISCLOSURE OF THE INVENTION

The present inventors have carried out extensive studies in order tosolve the aforementioned problems, and have found that, by incorporatingpyrrolidone or a derivative thereof, a polyhydric alcohol fatty acidester, and an organic acid in combination into a Pressure SensitiveAdhesive (PSA) containing diclofenac sodium, there can be produced apatch of a hydrophobic type which attains a consistently dissolved stateof diclofenac sodium in the PSA; exhibits excellent releasability ofdiclofenac sodium from the PSA and excellent percutaneous absorbabilityof diclofenac sodium; and exerts a stable analgesic anti-inflammatoryeffect for a long period of time.

Accordingly, the present invention provides an analgesicanti-inflammatory patch of a hydrophobic type for topical applicationcontaining, in a PSA, diclofenac sodium, pyrrolidone or a derivativethereof, a polyhydric alcohol fatty acid ester, and an organic acid.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a graph showing dissolution of diclofenac sodium contained intested patches.

FIG. 2 is a graph showing transdermal permeability of diclofenac sodiumreleased from tested patches.

BEST MODES FOR CARRYING OUT THE INVENTION

The patch of the present invention contains, in a PSA, diclofenacsodium, pyrrolidone or a derivative thereof, a polyhydric alcohol fattyacid ester, and an organic acid. As mentioned above, diclofenac sodiumis an active ingredient of the patch of the present invention.Preferably, diclofenac sodium is incorporated, as an active ingredient,into a PSA layer in an amount of 0.1-5.0 wt. %, more preferably 0.5-4.0wt. %. From another viewpoint, diclofenac sodium is preferablyincorporated into a PSA layer in an amount, per skin-contact area, of5-2,000 μg/cm², more preferably 50-400 μg/cm². In the context of thepresent invention, the “PSA layer” does not include the support; i.e.,the “PSA layer” refers to a layer containing the aforementionedingredients and other ingredients in the PSA.

Examples of the above pyrrolidone or derivative thereof include2-pyrrolidone and N-alkyl-2-pyrrolidones, with 2-pyrrolidone andN-methyl-2-pyrrolidone being particularly preferred. These pyrrolidoneand derivetives thereof function as a solubilizer for diclofenac sodium,and each pyrrolidone species is preferably incorporated into a PSA layerin an amount of 0.5-8.0 wt. %, more preferably 1.0-5.0 wt. %.

Examples of the polyhydric alcohol fatty acid ester include alcohol(dihydric to tetrahydric) fatty acid esters; e.g., glycerin fatty acidesters, ethylene glycol fatty acid esters, propylene glycol fatty acidesters, sorbitan fatty acid esters, and pentaerythritol fatty acidesters. Specific examples include glycerin mono-(C6-C18) fatty acidesters, ethylene glycol mono-(C6-C18) fatty acid esters, propyleneglycol mono-(C6-C18) fatty acid esters, sorbitan mono-(C6-C18) fattyacid esters, propylene glycol di-(C6-C18) fatty acid esters, andpentaerythritol tetra-(C6-C18) fatty acid esters. Of these, glycerinfatty acid esters (e.g., glyceryl tri(caprylate•caprate)), ethyleneglycol fatty acid esters, pentaerythritol fatty acid ester (e.g.,pentaerythrityl tetra-2-ethylhexanoate), and propylene glycol fatty acidesters (e.g., propylene glycol monocaprylate and propylene glycoldicaprylate) are more preferred. Of these, propylene glycol fatty acidesters are still more preferred. Examples of commercial products ofthese esters include Sefsol (product of Nikko Chemicals Co., Ltd.).These polyhydric alcohol fatty acid esters function as a percutaneousabsorption promoter for diclofenac sodium and may be used in combinationof two or more species. The ester is preferably incorporated into a PSAlayer in an amount of 0.2-10.0 wt. %, more preferably 0.5-5.0 wt. %.

Examples of the organic acid include C3-C6 dicarboxylic acids and C3-C6tricarboxylic acids. Of these, citric acid, tartaric acid, and succinicacid are preferred. These organic acids function as percutaneousabsorption promoters for diclofenac sodium and may be used incombination of two or more species. The organic acid is preferablyincorporated into a PSA layer in an amount of 0.05-4.0 wt. %, morepreferably 0.1-2.0 wt. %.

As mentioned above, both the polyhydric alcohol fatty acid ester and theorganic acid function as percutaneous absorption promoters fordiclofenac sodium. The ratio by weight of the polyhydric alcohol fattyacid ester to the organic acid preferably falls within a range of 1:20to 200:1, more preferably 1:4 to 50:1. The total amount of thepolyhydric alcohol fatty acid ester and the organic acid incorporatedinto a PSA layer preferably falls within a range of 0.25-14 wt. %, morepreferably 0.6-7 wt. %.

The PSA into which the above components are to be incorporated is formedfrom a PSA base and a tackifier in combination. A preferable PSA base isa styrene-isoprene-styrene block copolymer (SIS). The SIS iscommercially available, and examples of commercial products includeCariflex TR-1107 and Cariflex TR-1117 (trade names; product of ShellKagaku K.K.). The amount of the PSA base incorporated into a PSA layerpreferably falls within a range of 10-50 wt. %, more preferably 10-40wt. %.

Examples of the tackifier include rosin ester resin, polyterpene resin,terpene phenol resin, and petroleum resin. Of these, rosin ester resinis preferred, with a rosin ester resin which has been subjected toremoval of low-boiling fractions and subsequent hydrogenation (e.g.,Ester Gum HG, product of Arakawa Chemical Industries, Ltd.) beingparticularly preferred. YS Resin (polyterpene resin, product of YasuharaYushi Kogyo Co., Ltd.), YS Polyster (terpene phenol resin, product ofYasuhara Yushi Kogyo Co., Ltd.), Quintone (petroleum resin, product ofNippon Zeon Co., Ltd.), Arkon (petroleum resin, product of ArakawaChemical Industries, Ltd.), Escorez (petroleum resin, product of ExxonCorp.), and other similar products may be used. The amount of thetackifier incorporated into a PSA layer preferably falls within a rangeof 5-50 wt. %, more preferably 5-30 wt. %.

The patch of the present invention may further contain arbitrarycomponents such as an essential oil component (e.g., 1-menthol or menthaoil); a softening agent (e.g., liquid paraffin); an antiageing agent; ora filler (inorganic compound). In addition to diclofenac sodium, thepatch of the present invention may further contain another drugcomponent such as ketoprofen, indomethacin, flurbiprofen, glycolylsalicylate, methyl salicylate, capsaicine, nonyl vanillylamide,tocopheryl acetate, a phellodendron bark extract, or an AesculusHippocastanum Seed extract. The softening agent is preferablyincorporated into a PSA layer in an amount of 30-70 wt. %, morepreferably 40-60 wt. %. The essential oil component is preferablyincorporated into a PSA layer in an amount of 0.2-5.0 wt. %, morepreferably 0.5-3.0 wt. %.

As mentioned above, the PSA layer included in the patch of the presentinvention is of hydrophobic type and contains substantially no water.This feature renders the present invention fundamentally different fromthat of conventional cataplasms.

The patch of the present invention can be produced by spreading theaforementioned PSA base on a soft support. Any type of support can beemployed so long as the support is formed of a soft sheet which does notpermit permeation of the PSA base through the back of the support.Examples of the sheet employable as the support of the present inventioninclude woven and non-woven fabrics; plastic films such as polyolefinfilm, polyvinyl alcohol film, vinyl chloride film, urethane alloy film,urethane-vinyl chloride copolymer film, and ethylene-vinyl acetate film;film of a foamed blend of acrylic polymer or polystyrene-polybutadieneand polyisoprene; these films on which metal is coated through vapordeposition; and laminated sheets obtained from two or more species ofthese films. Appropriately, the support typically has a thickness ofabout 1,000 μm or less, preferably 30-700 μm.

The thus-produced patch of the present invention is applied to skinsites where an analgesic anti-inflammatory effect is needed; e.g.,inflammation sites of the joints, muscles, neck, etc.

EXAMPLES

The present invention will next be described in more detail by way ofexamples, which should not be construed as limiting the inventionthereto.

Examples 1 to 4

In each example, a PSA base and a softening agent shown in Table 1 werekneaded by use of a heating-kneader. A tackifier was added to thekneaded product, and the resultant mixture was further kneaded.Subsequently, diclofenac sodium was dissolved in a liquid mixturecontaining pyrrolidone, a polyhydric alcohol fatty acid ester, andcitric acid, and the resultant solution was added to the above kneadedproduct. The resultant mixture was further kneaded, to thereby yield auniform mixture. The mixture was applied to and spread on a support, tothereby form a PSA layer. After an appropriate period of time, the PSAlayer was covered with a liner, and the resultant laminated product wascut into pieces of desired dimensions, to thereby obtain patches.

TABLE 1 (wt. %) Ex. 1 Ex. 2 Ex. 3 Ex. 4 PSA base SIS 28.5 28.5 38.0 30.0Polyisobutylene  2.0 — —  4.0 Tackifier Ester Gum HG*¹ 12.0 12.0 20.025.0 Softening agent Liquid paraffin 50.1 50.1 33.8 32.7 Solubilizer2-Pyrrolidone  4.0  4.0  2.0  1.0 Absorption promoter Sefsol*²  2.0  2.0 4.0  3.0 Citric acid  0.4  0.4  0.2  0.3 Tackiness regulator 1-Menthol 2.0  1.0  3.0 Drug ingredient Diclofenac sodium  1.0  1.0  1.0  1.0^(*1)Hydrogenated rosin ester resin (Arakawa Chemical Industries, Ltd.)^(*2)Glycerin fatty acid ester (Nikko Chemicals Co., Ltd.)

Test Example 1 Dissolution Test

The time-elapsed dissolution amount of diclofenac sodium released fromeach patch was determined through a paddle over disk method by use of adissolution tester according to Japanese Pharmacopoeia. Specifically,each test patch was cut into pieces (5 cm×5 cm), and each piece wasbonded to Teflon mesh. The piece was clamped by two pieces of watchglass and placed in a phosphate buffer (900 mL, pH: 7.2) at 32° C. Apaddle was rotated 25 mm above the patch, and a liquid (1 mL) wassampled at an intermediate level between the bottom of the paddle andthe liquid surface. The sampling was performed 0.5, 1, 2, 3, 4, 6, and 8hours after paddle rotation. Diclofenac sodium contained in each sampledliquid was quantitated through high performance liquid chromatography.

The patches prepared in the above Examples 1 to 4 and those prepared inComparative Examples were employed as test patches. Test patches ofComparative Examples were prepared in accordance with the formulationsshown in Table 2 in a manner similar to those employed in Examples 1 to4.

TABLE 2 (wt.%) Comp. Comp. Comp. Comp. Comp. Comp. Ex. 1 Ex. 2 Ex. 3 Ex.4 Ex. 5 Ex. 6 SIS 28.5 28.5 28.5 28.5 28.5 28.5 Polyiso-  2.0  2.0  2.0 2.0 — — butylene Ester Gum HG 12.0 12.0 12.0 12.0 12.0 12.0 Liquidparaffin 54.0 50.0 54.5 56.1 58.5 52.5 Pyrrolidone —  4.0 — — —  4.0Sefsol — —  2.0 — —  2.0 Citric acid — — —  0.4 — — 1-Menthol  2.5  2.5— — — — Diclofenac Na  1.0  1.0  1.0  1.0  1.0  1.0 Comp. Ex. 1: Patchdisclosed in Japanese Patent Applicatian Laid-Open (kokai) No. 4-198326Comp. Ex. 2: Patch disclosed in Japanese Patent Application Laid-Open(kokai) No. 11-222443 Comp. Ex. 3: Patch disclosed in Japanese PatentApplication Laid-Open (kokai) No. 5-178763 Comp. Ex. 4: Patch disclosedin Japanese Patent Application Laid-Open (kokai) No. 61-280426

Each of the thus-determined diclofenac sodium levels was converted tothe corresponding percent dissolution from the patch (%). The resultsare shown in FIG. 1. In FIG. 1, “Mean,” “SD,” and “n” denote a meanvalue, a standard deviation, and the number of test samples,respectively.

The results indicate that the patches according to the present inventionexhibit percent dissolution as high as four times or more that of allpatches of Comparative Examples 1 to 6.

Test Example 2 Transdermal Permeability Test

Hairless rats (body weight: 170 g) were anesthetized by pentobarbital.After removal of hair from the abdomen, abdominal skin samples wereextirpated. Each of the thus-extirpated skin samples was set in avertical cell (effective permeation area: 2.83 cm², cell capacity: 16mL), and a test patch (diameter: 1.9 cm) was attached to the skinsample. Subsequently, the receiver liquid in the cell was stirred bymeans of an electromagnetic stirrer while the cell was heated at 37° C.A portion (0.5 mL) of the receiver liquid was sampled a plurality oftimes at constant time intervals, and the diclofenac sodium content ofthe liquid portion was determined.

FIG. 2 shows cumulative permeation amounts of diclofenac sodium that hadbeen released from each patch sample and had permeated each extirpatedskin sample of the abdomen of each rat (Examples 1 and 2 and ComparativeExamples 1 to 6). As is clear from FIG. 2, the patches according to thepresent invention exhibit cumulative permeation amounts as high as aboutthree times or more those of patches of Comparative Examples 1 to 6.

The results of Test Examples 1 and 2 indicate that the patch of thepresent invention can exhibit remarkably promoted releasability andpercutaneous absorbability of diclofenac sodium which conventionaltechniques have not satisfactorily attained. Thus, the patch of thepresent invention has proven to be a clinically useful patch whichmitigates systemic adverse effect and provides other advantages.

INDUSTRIAL APPLICABILITY

The patch of the present invention exerts the following effects:

(1) diclofenac sodium is effectively and continuously released from aPSA and percutaneously absorbed, thereby attaining sustained, excellentpharmaceutical and pharmacological effects;

(2) the patch per se has high tackiness and safety; and

(3) diclofenac sodium remains stable in the PSA.

1. An analgesic anti-inflammatory Pressure Sensitive Adhesive (PSA)patch fox topical application, comprising a soft support and a PSA layeron the soft support, wherein the PSA layer comprises 1 wt. % ofdiclofenac sodium, 2 to 4 wt. % of N-methyl-2-pyrrolidone, 2 wt. % ofpropylene glycol monocaprylate, 0.4 wt % of citric acid, 28.5 to 38 wt %of a styrene-isoprene-styrene block copolymer, 2 to 4 wt %polyisobutylene, 12 to 25 wt % of an ester gum, 30 to 40 wt % of liquidparaffin, and no added water.
 2. The patch of claim 1, wherein the PSAlayer further comprises l-menthol.
 3. The patch of claim 1, wherein thePSA layer contains 1 to 3 wt. % of the l-menthol.
 4. The patch of claim1, wherein the PSA layer contains no l-menthol.
 5. The patch of claim 1,further comprising an anti-ageing agent.
 6. The patch of claim 1,wherein the soft support does not permit permeation of the PSA layerthrough the back of the support.
 7. The patch of claim 1, wherein thesoft support is selected from the group consisting of woven fabrics,non-woven fabrics, plastic films, and films of a foamed blend of acrylicpolymer or polystyrene-polybutadiene and polyisoprene.
 8. The parch ofclaim 1, wherein the soft support is a plastic film selected from thegroup consisting of polyolefin film, polyvinyl alcohol film, vinylchloride film, urethane alloy film, urethane-vinyl chloride copolymerfilm, and ethylene-vinyl acetate film.
 9. The patch of claim 8, whereinthe film is selected from the group consisting of plastic films, andfilms of a foamed blend of acrylic polymer or polystyrene-polybutadieneand polyisoprene.
 10. The patch of claim 1, wherein the soft support hasa thickness of about 1,000 μm or less.
 11. The patch of claim 1, whereinthe soft support has a thickness of 30-700 μm.